An aptamer-based biosensor for colorimetric detection of Escherichia coli O157:H7.

BACKGROUND: An aptamer based biosensor (aptasensor) was developed and evaluated for rapid colorimetric detection of Escherichia coli (E. coli) O157:H7. METHODOLOGY/PRINCIPAL FINDINGS: The aptasensor was assembled by modifying the truncated lipopolysaccharides (LPS)-binding aptamer on the surface of...

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Main Authors: Wenhe Wu, Jie Zhang, Meiqin Zheng, Yuhong Zhong, Jie Yang, Yuhong Zhao, Wenping Wu, Wei Ye, Jie Wen, Qi Wang, Jianxin Lu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3492178?pdf=render
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author Wenhe Wu
Jie Zhang
Meiqin Zheng
Yuhong Zhong
Jie Yang
Yuhong Zhao
Wenping Wu
Wei Ye
Jie Wen
Qi Wang
Jianxin Lu
author_facet Wenhe Wu
Jie Zhang
Meiqin Zheng
Yuhong Zhong
Jie Yang
Yuhong Zhao
Wenping Wu
Wei Ye
Jie Wen
Qi Wang
Jianxin Lu
author_sort Wenhe Wu
collection DOAJ
description BACKGROUND: An aptamer based biosensor (aptasensor) was developed and evaluated for rapid colorimetric detection of Escherichia coli (E. coli) O157:H7. METHODOLOGY/PRINCIPAL FINDINGS: The aptasensor was assembled by modifying the truncated lipopolysaccharides (LPS)-binding aptamer on the surface of nanoscale polydiacetylene (PDA) vesicle using peptide bonding between the carboxyl group of the vesicle and the amine group of the aptamer. Molecular recognition between E. coli O157:H7 and aptamer at the interface of the vesicle lead to blue-red transition of PDA which was readily visible to the naked eyes and could be quantified by colorimetric responses (CR). Confocal laser scanning microscope (CLSM) and transmission electron microscopy (TEM) was used to confirm the specific interactions between the truncated aptamer and E. coli O157:H7. The aptasensor could detect cellular concentrations in a range of 10(4)~ 10(8) colony-forming units (CFU)/ml within 2 hours and its specificity was 100% for detection of E. coli O157:H7. Compared with the standard culture method, the correspondent rate was 98.5% for the detection of E. coli O157:H7 on 203 clinical fecal specimens with our aptasensor. CONCLUSIONS: The new aptasensor represents a significant advancement in detection capabilities based on the combination of nucleic acid aptamer with PDA vesicle, and offers a specific and convenient screening method for the detection of pathogenic bacteria. This technic could also be applied in areas from clinical analysis to biological terrorism defense, especially in low-resource settings.
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spelling doaj.art-4f3b1af1d64a482591513cb551536baf2022-12-21T18:32:47ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01711e4899910.1371/journal.pone.0048999An aptamer-based biosensor for colorimetric detection of Escherichia coli O157:H7.Wenhe WuJie ZhangMeiqin ZhengYuhong ZhongJie YangYuhong ZhaoWenping WuWei YeJie WenQi WangJianxin LuBACKGROUND: An aptamer based biosensor (aptasensor) was developed and evaluated for rapid colorimetric detection of Escherichia coli (E. coli) O157:H7. METHODOLOGY/PRINCIPAL FINDINGS: The aptasensor was assembled by modifying the truncated lipopolysaccharides (LPS)-binding aptamer on the surface of nanoscale polydiacetylene (PDA) vesicle using peptide bonding between the carboxyl group of the vesicle and the amine group of the aptamer. Molecular recognition between E. coli O157:H7 and aptamer at the interface of the vesicle lead to blue-red transition of PDA which was readily visible to the naked eyes and could be quantified by colorimetric responses (CR). Confocal laser scanning microscope (CLSM) and transmission electron microscopy (TEM) was used to confirm the specific interactions between the truncated aptamer and E. coli O157:H7. The aptasensor could detect cellular concentrations in a range of 10(4)~ 10(8) colony-forming units (CFU)/ml within 2 hours and its specificity was 100% for detection of E. coli O157:H7. Compared with the standard culture method, the correspondent rate was 98.5% for the detection of E. coli O157:H7 on 203 clinical fecal specimens with our aptasensor. CONCLUSIONS: The new aptasensor represents a significant advancement in detection capabilities based on the combination of nucleic acid aptamer with PDA vesicle, and offers a specific and convenient screening method for the detection of pathogenic bacteria. This technic could also be applied in areas from clinical analysis to biological terrorism defense, especially in low-resource settings.http://europepmc.org/articles/PMC3492178?pdf=render
spellingShingle Wenhe Wu
Jie Zhang
Meiqin Zheng
Yuhong Zhong
Jie Yang
Yuhong Zhao
Wenping Wu
Wei Ye
Jie Wen
Qi Wang
Jianxin Lu
An aptamer-based biosensor for colorimetric detection of Escherichia coli O157:H7.
PLoS ONE
title An aptamer-based biosensor for colorimetric detection of Escherichia coli O157:H7.
title_full An aptamer-based biosensor for colorimetric detection of Escherichia coli O157:H7.
title_fullStr An aptamer-based biosensor for colorimetric detection of Escherichia coli O157:H7.
title_full_unstemmed An aptamer-based biosensor for colorimetric detection of Escherichia coli O157:H7.
title_short An aptamer-based biosensor for colorimetric detection of Escherichia coli O157:H7.
title_sort aptamer based biosensor for colorimetric detection of escherichia coli o157 h7
url http://europepmc.org/articles/PMC3492178?pdf=render
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